Pediatric split liver transplantation after Fontan procedure in left isomerism combined with biliary atresia: A case report

被引:5
作者
Youn, Joong Kee [1 ]
Lee, Jeong-Moo [1 ]
Yi, Nam-Joon [1 ]
Choi, Young Rok [1 ]
Suh, Suk-Won [1 ]
You, Tae [1 ]
Lee, Kwang-Woong [1 ]
Jung, Chul-Woo [2 ]
Lee, Ji-won [2 ]
Bae, Eun-Jung [3 ]
Ko, Jae Sung [3 ]
Kim, Woong-Han [4 ]
Park, Kwi-Won [1 ]
Suh, Kyung-Suk [1 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Surg, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Anesthisiol & Pain Med, Seoul 110744, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Pediat, Seoul 110744, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Thorac Surg, Seoul 110744, South Korea
关键词
biliary atresia; left isomerism; Fontan operation; hepatopulmonary syndrome; liver transplantation; SITUS-INVERSUS; HEPATOPULMONARY SYNDROME; OPERATION; MORTALITY; SURGERY; COMPLICATIONS; CIRCULATION; PREDICTORS; OUTCOMES; CHILDREN;
D O I
10.1111/petr.12364
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
LI is a subset of the heterotaxy syndrome and a rare birth defect that involves the heart and other organs. It can be combined with extracardiac abnormalities, especially BA. CHD can be associated with LI in up to 15% of cases, although it is rare in BA. Pediatric LT for a child with ESLD due to BA combined with LI and CHD is a challenging issue for a transplant surgeon. Herein, we report a successful split LT on a three-yr-old boy with LI who survived after a Fontan procedure due to single ventricle, but who suffered from HPS associated with BA.
引用
收藏
页码:E274 / E279
页数:6
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